Enrichment of ovine gonadotropes via adenovirus gene targeting enhances assessment of transcriptional changes in response to estradiol-17 beta

Gonadotropes represent approximately 5–15% of the total endocrine cell population in the mammalian anterior pituitary. Therefore, assessing the effects of experimental manipulation on virtually any parameter of gonadotrope biology is difficult to detect and parse from background noise. In non-rodent...

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Veröffentlicht in:Biology of reproduction 2020-02, Vol.102 (1), p.156-169
Hauptverfasser: Murtazina, Dilyara A, Arreguin-Arevalo, Jesus Alejandro, Cantlon, Jeremy D, Ebrahimpour-Boroojeny, Ali, Shrestha, Akash, Hicks, Jennifer A, Magee, Christianne, Kirkley, Kelly, Jones, Kenneth, Nett, Terry M, Chitsaz, Hamidreza, Clay, Colin M
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container_end_page 169
container_issue 1
container_start_page 156
container_title Biology of reproduction
container_volume 102
creator Murtazina, Dilyara A
Arreguin-Arevalo, Jesus Alejandro
Cantlon, Jeremy D
Ebrahimpour-Boroojeny, Ali
Shrestha, Akash
Hicks, Jennifer A
Magee, Christianne
Kirkley, Kelly
Jones, Kenneth
Nett, Terry M
Chitsaz, Hamidreza
Clay, Colin M
description Gonadotropes represent approximately 5–15% of the total endocrine cell population in the mammalian anterior pituitary. Therefore, assessing the effects of experimental manipulation on virtually any parameter of gonadotrope biology is difficult to detect and parse from background noise. In non-rodent species, applying techniques such as high-throughput ribonucleic acid (RNA) sequencing is problematic due to difficulty in isolating and analyzing individual endocrine cell populations. Herein, we exploited cell-specific properties inherent to the proximal promoter of the human glycoprotein hormone alpha subunit gene (CGA) to genetically target the expression of a fluorescent reporter (green fluorescent protein [GFP]) selectively to ovine gonadotropes. Dissociated ovine pituitary cells were cultured and infected with an adenoviral reporter vector (Ad-hαCGA-eGFP). We established efficient gene targeting by successfully enriching dispersed GFP-positive cells with flow cytometry. Confirming enrichment of gonadotropes specifically, we detected elevated levels of luteinizing hormone (LH) but not thyrotropin-stimulating hormone (TSH) in GFP-positive cell populations compared to GFP-negative populations. Subsequently, we used next-generation sequencing to obtain the transcriptional profile of GFP-positive ovine gonadotropes in the presence or absence of estradiol 17-beta (E2), a key modulator of gonadotrope function. Compared to non-sorted cells, enriched GFP-positive cells revealed a distinct transcriptional profile consistent with established patterns of gonadotrope gene expression. Importantly, we also detected nearly 200 E2-responsive genes in enriched gonadotropes, which were not apparent in parallel experiments on non-enriched cell populations. From these data, we conclude that CGA-targeted adenoviral gene transfer is an effective means for selectively labeling and enriching ovine gonadotropes suitable for investigation by numerous experimental approaches. Summary sentence Unique RNA signatures establish the efficacy of combining adenovirus-mediated gene transfer and flow cytometry to isolate an enriched population of gonadotrope cells from the ovine pituitary gland.
doi_str_mv 10.1093/biolre/ioz166
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Therefore, assessing the effects of experimental manipulation on virtually any parameter of gonadotrope biology is difficult to detect and parse from background noise. In non-rodent species, applying techniques such as high-throughput ribonucleic acid (RNA) sequencing is problematic due to difficulty in isolating and analyzing individual endocrine cell populations. Herein, we exploited cell-specific properties inherent to the proximal promoter of the human glycoprotein hormone alpha subunit gene (CGA) to genetically target the expression of a fluorescent reporter (green fluorescent protein [GFP]) selectively to ovine gonadotropes. Dissociated ovine pituitary cells were cultured and infected with an adenoviral reporter vector (Ad-hαCGA-eGFP). We established efficient gene targeting by successfully enriching dispersed GFP-positive cells with flow cytometry. Confirming enrichment of gonadotropes specifically, we detected elevated levels of luteinizing hormone (LH) but not thyrotropin-stimulating hormone (TSH) in GFP-positive cell populations compared to GFP-negative populations. Subsequently, we used next-generation sequencing to obtain the transcriptional profile of GFP-positive ovine gonadotropes in the presence or absence of estradiol 17-beta (E2), a key modulator of gonadotrope function. Compared to non-sorted cells, enriched GFP-positive cells revealed a distinct transcriptional profile consistent with established patterns of gonadotrope gene expression. Importantly, we also detected nearly 200 E2-responsive genes in enriched gonadotropes, which were not apparent in parallel experiments on non-enriched cell populations. From these data, we conclude that CGA-targeted adenoviral gene transfer is an effective means for selectively labeling and enriching ovine gonadotropes suitable for investigation by numerous experimental approaches. Summary sentence Unique RNA signatures establish the efficacy of combining adenovirus-mediated gene transfer and flow cytometry to isolate an enriched population of gonadotrope cells from the ovine pituitary gland.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1093/biolre/ioz166</identifier><identifier>PMID: 31504222</identifier><language>eng</language><publisher>United States: Society for the Study of Reproduction</publisher><subject>Adenoviridae ; Adenoviruses ; Animals ; anterior pituitary ; Biology ; Estradiol ; Estradiol - pharmacology ; Flow cytometry ; Gene expression ; Genetic aspects ; Genetic engineering ; Glycoproteins ; Gonadotrophs - drug effects ; Gonadotrophs - metabolism ; gonadotropin-releasing hormone (GnRH/GnRH receptor): ovine/sheep ; Luteinizing Hormone - metabolism ; Physiological aspects ; Pituitary gland ; Pituitary Gland, Anterior - drug effects ; Pituitary Gland, Anterior - metabolism ; Proteins ; Reproductive health ; RESEARCH ARTICLE ; Sheep ; Thyrotropin - metabolism ; transcription</subject><ispartof>Biology of reproduction, 2020-02, Vol.102 (1), p.156-169</ispartof><rights>The Author(s) 2019. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com journals.permissions@oup.com</rights><rights>The Author(s) 2019. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2019</rights><rights>The Author(s) 2019. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><rights>The Author(s) 2019. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. 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Confirming enrichment of gonadotropes specifically, we detected elevated levels of luteinizing hormone (LH) but not thyrotropin-stimulating hormone (TSH) in GFP-positive cell populations compared to GFP-negative populations. Subsequently, we used next-generation sequencing to obtain the transcriptional profile of GFP-positive ovine gonadotropes in the presence or absence of estradiol 17-beta (E2), a key modulator of gonadotrope function. Compared to non-sorted cells, enriched GFP-positive cells revealed a distinct transcriptional profile consistent with established patterns of gonadotrope gene expression. Importantly, we also detected nearly 200 E2-responsive genes in enriched gonadotropes, which were not apparent in parallel experiments on non-enriched cell populations. From these data, we conclude that CGA-targeted adenoviral gene transfer is an effective means for selectively labeling and enriching ovine gonadotropes suitable for investigation by numerous experimental approaches. 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Therefore, assessing the effects of experimental manipulation on virtually any parameter of gonadotrope biology is difficult to detect and parse from background noise. In non-rodent species, applying techniques such as high-throughput ribonucleic acid (RNA) sequencing is problematic due to difficulty in isolating and analyzing individual endocrine cell populations. Herein, we exploited cell-specific properties inherent to the proximal promoter of the human glycoprotein hormone alpha subunit gene (CGA) to genetically target the expression of a fluorescent reporter (green fluorescent protein [GFP]) selectively to ovine gonadotropes. Dissociated ovine pituitary cells were cultured and infected with an adenoviral reporter vector (Ad-hαCGA-eGFP). We established efficient gene targeting by successfully enriching dispersed GFP-positive cells with flow cytometry. Confirming enrichment of gonadotropes specifically, we detected elevated levels of luteinizing hormone (LH) but not thyrotropin-stimulating hormone (TSH) in GFP-positive cell populations compared to GFP-negative populations. Subsequently, we used next-generation sequencing to obtain the transcriptional profile of GFP-positive ovine gonadotropes in the presence or absence of estradiol 17-beta (E2), a key modulator of gonadotrope function. Compared to non-sorted cells, enriched GFP-positive cells revealed a distinct transcriptional profile consistent with established patterns of gonadotrope gene expression. Importantly, we also detected nearly 200 E2-responsive genes in enriched gonadotropes, which were not apparent in parallel experiments on non-enriched cell populations. From these data, we conclude that CGA-targeted adenoviral gene transfer is an effective means for selectively labeling and enriching ovine gonadotropes suitable for investigation by numerous experimental approaches. Summary sentence Unique RNA signatures establish the efficacy of combining adenovirus-mediated gene transfer and flow cytometry to isolate an enriched population of gonadotrope cells from the ovine pituitary gland.</abstract><cop>United States</cop><pub>Society for the Study of Reproduction</pub><pmid>31504222</pmid><doi>10.1093/biolre/ioz166</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenoviridae
Adenoviruses
Animals
anterior pituitary
Biology
Estradiol
Estradiol - pharmacology
Flow cytometry
Gene expression
Genetic aspects
Genetic engineering
Glycoproteins
Gonadotrophs - drug effects
Gonadotrophs - metabolism
gonadotropin-releasing hormone (GnRH/GnRH receptor): ovine/sheep
Luteinizing Hormone - metabolism
Physiological aspects
Pituitary gland
Pituitary Gland, Anterior - drug effects
Pituitary Gland, Anterior - metabolism
Proteins
Reproductive health
RESEARCH ARTICLE
Sheep
Thyrotropin - metabolism
transcription
title Enrichment of ovine gonadotropes via adenovirus gene targeting enhances assessment of transcriptional changes in response to estradiol-17 beta
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